Increased basal water and food ingestion in cingulectomized rats

Psychonomic Science, Mar 2014

Rats with anterior cingulate lesions showed a sustained mean increase of 22% in water ingestion. They also showed an immediate postoperative decrease of 30% in food intake followed by a prolonged elevation of 8%. Sham operated, cortical control subjects, and normal animals did not show any changes in food or water ingestion.

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Increased basal water and food ingestion in cingulectomized rats

• Increased basal water and food ingestion In cingulectomized rats 1 J. F. Lohar and J. W. Wolle UNIVERSITY OF ROCHESTER Abstract Rats with anterior cingulate lesions showed a sustained mean increase of 22% in water ingestion. They also showed an immediate postoperative decrease of 30% in food intake followed by a prolonged elevation of 8%. Sham operated, cortical control subjects, and normal animals did not show any changes in food or water ingestion. ProblelD Previous studies by McCleary (1961) and Kaada et al. (1962) have shown that rats and cats with septal lesions are deficient in inhibiting approach responses to food or water through which shock punishment is delivered. In contrast, lesions ofthe cingulate cortex do not disrupt such passive-avoidance behavior, and in cats produce a stronger avoidance response than that obtained from unoperated subjects (Lubar, 1964). Because the passive avoidance of food or water involves the withholding of a consummatory response, it is important to determine whether the motivational state of animals is changed by the medial cortical lesions described above. There is recent evidence that rats with electrolytically placed septal lesions show increased water consumption and faster lever pressing for water reinforcement on CRF and FI operant schedules (Hunt & Harvey, 1964). One could argue from this data that the passive-avoidance deficits in septal Ss arises from an increased thirst drive. However, if cingulectomized animals also show increases in food and water consump,tion, the hypothesis that medial cortical lesions produce changes in alimentary drive state consistent with their passive-avoidance performance would be less tenable than the response hypothesis proposed by McCleary (1961). We predicted that cingulate lesions would increase alimentary ingestion. This was based on observations that cingulectomized cats eat and drink more than do normal Ss during training in the passive-avoidance apparatus, prior to shock administration. Method The Ss were 17 Sprague-Dawley rats (380-460 gm), 120 days old at the beginningofthe experiment. Ss were randomly subdivided into an experimental group of seven cingulectomized animals and a control group consisting of three sham operates, two cortical controls, and five normal controls. Each S was housed in an individual cage. The room temperature was maintained between 22 0 C-25.5 0 C, and the humidity was kept constant. Ss were fed on an ad libitum ingestion schedule. Food conSisted of a wet mash, 38% Purina Micromix Rat Chow and 62% tap water, by weight, placed in ointment jars. Aychon. Sci., 1964, Vol. 1. Water evaporation from the mash was negligible. Water was provided in 250 ml stopped bottles attached to each cage, and was obtained by S through a metal spout. There was no problem with leakage. Measurements of the quantities of water and food ingested were made at the same hour each day. These were begun several weeks after the animals had arrived in the laboratory and were taken for a minmum of from eight days preoperatively until the termination of the experiment, 48 days postoperatively. The procedure was was as follows: For water, each bottle was filled to a specified level, weighed to 0.5 gm, and attached to the S's cage. After 24 hours, it was weighed again, and the amount of water consumed was recorded. The bottle was then washed, refilled and replaced on the cage for the next day's measurement. Food consumption was measured in a similar fashion. In addition, each animal was weighed every two days. Surgery was done aseptically by aspiration and was completed within an eight-day period. The anesthetic used was sodium pentobarbitol (.08 cc/100 gm body weight of 60 mg/cc solution Nembutal) supplemented by ether. Cingulate cortex was removed bilaterally, from 1.0 mm posterior to the bregma to the olfactory bulbs, without any interruption of the superior sagittal sinus. Cortical lesions were made laterally and were comparable to the cingulectomies in the amount of tissue removed. Sham operations consisted of bilateral dural incisions at the level of the anterior cingulate cortex. Subsequent histology revealed that none of the lesions invaded the septal area. Resnlts The results are shown in Fig. 1. Amounts of water and food consumed are plotted in ml andgm per 100 gm of body weight, respectively. These are more appropriate measures, due to weight differences among animals, than are total amounts ingested. The measurements of water ingested included measures of tap water from the bottles and water contained in the wet food mash. Similarly, the amount of food eaten was calculated on the basis of the amount of dry food contained in the wet mash. Compared to the control group, animals with cingulate lesions showed a rapid increase in daily water ingestion which reached a mean maximum of 32%, two to three weeks postoperatively. Since the sham operated subjects and cortical controls showed no Significant changes in either water or food ingestion postopera~ tively (p > .50, Mann-Whitney U-test), their data was pooled with that of the normal controls. Throughout the 289 SURGERY ~ 16 ~ 15 >- "'O--._--.o..~, 81 W In a:: '''o-. __-o...'''''''4Y""A • I f- ~~ 0 1 o 'II ...J ::!: o,~ __ ~~ _________________________________ ....., CINGULATES ...... CONTROLS o o ~ ---0."" 3 4 5 6 7 8 9 10 4 DAY BLOCKS " 12 13 14 Fig. 1. Water and food ingestion in cingulectomized (N ~ 7) and control animals (sham operates, cortical controls and normal animals, N=10). course of the experiment, the cingulate lesion and control groups showed parallel rates of change in water ingestion. The cingulate lesion group attained a mean increase in water ingestion of 22%, over the entire postoperative period, compared with the controls. This increase is statistically Significant resulting in a U = 7; df, 7/10; p< .01 (Mann-Whitney U-test, two-tail). Even 48 days postoperatively, these Ss were daily consuming 25% more water than the control groups. Furthermore, compared to their base preoperative levels, individual Ss with cingulate lesions showed maximal postoperative increases in water ingestion (over a single four-day period) ranging from 5.1% to 39%, whereas the control group showed a slow and steady decrease in water intake (per 100 gm of body weight) compared to their base preoperative or initial levels. The small parallel decrease in water ingestion for both groups, during the course of the experiment, probably reflects an overall diminution of water consumed per unit body weight as Ss reached maturity. Significant differences in water ingestion between the cingulate and control groups cannot be attributed to differences in body weight between the two groups since the latter was not significantly different (p > .50, Mann-Whitney U-test). Based on the evidence presented, we suggest that the effect of the cingulate lesion on water ingestion is long-term and perhaps permanent. The cingule (...truncated)


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J. F. Lubar, J. W. Wolfe. Increased basal water and food ingestion in cingulectomized rats, Psychonomic Science, 2014, pp. 289-290, Volume 1, Issue 1-12, DOI: 10.3758/BF03342917